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Escitalopram Oxalate - 51672-1348-1 - (Escitalopram Oxalate)

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Drug Information of Escitalopram Oxalate

Product NDC: 51672-1348
Proprietary Name: Escitalopram Oxalate
Non Proprietary Name: Escitalopram Oxalate
Active Ingredient(s): 5    mg/5mL & nbsp;   Escitalopram Oxalate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Escitalopram Oxalate

Product NDC: 51672-1348
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079121
Marketing Category: ANDA
Start Marketing Date: 20120503

Package Information of Escitalopram Oxalate

Package NDC: 51672-1348-1
Package Description: 1 BOTTLE in 1 CARTON (51672-1348-1) > 240 mL in 1 BOTTLE

NDC Information of Escitalopram Oxalate

NDC Code 51672-1348-1
Proprietary Name Escitalopram Oxalate
Package Description 1 BOTTLE in 1 CARTON (51672-1348-1) > 240 mL in 1 BOTTLE
Product NDC 51672-1348
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram Oxalate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20120503
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name ESCITALOPRAM OXALATE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Escitalopram Oxalate


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